Jordi Burés

3.0k total citations
49 papers, 2.5k citations indexed

About

Jordi Burés is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Jordi Burés has authored 49 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Organic Chemistry, 21 papers in Inorganic Chemistry and 17 papers in Molecular Biology. Recurrent topics in Jordi Burés's work include Asymmetric Synthesis and Catalysis (19 papers), Asymmetric Hydrogenation and Catalysis (16 papers) and Synthesis and Catalytic Reactions (12 papers). Jordi Burés is often cited by papers focused on Asymmetric Synthesis and Catalysis (19 papers), Asymmetric Hydrogenation and Catalysis (16 papers) and Synthesis and Catalytic Reactions (12 papers). Jordi Burés collaborates with scholars based in United Kingdom, Spain and United States. Jordi Burés's co-authors include Donna G. Blackmond, Alan Armstrong, Christian D.‐T. Nielsen, Igor Larrosa, Jaume Vilarrasa, Daniel Whitaker, Enrique Gómez‐Bengoa, Lillian V. A. Hale, Rosie J. Somerville and Rubén Martı́n and has published in prestigious journals such as Nature, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Jordi Burés

48 papers receiving 2.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Jordi Burés United Kingdom 24 2.0k 780 452 237 191 49 2.5k
Taku Kitanosono Japan 23 1.9k 0.9× 586 0.8× 435 1.0× 246 1.0× 204 1.1× 47 2.2k
Carlos Silva López Spain 29 1.8k 0.9× 410 0.5× 356 0.8× 215 0.9× 98 0.5× 114 2.4k
Stephan J. Zuend United States 14 1.4k 0.7× 511 0.7× 387 0.9× 125 0.5× 150 0.8× 16 1.7k
Christine Fischer Germany 30 2.5k 1.3× 1.0k 1.3× 506 1.1× 204 0.9× 288 1.5× 154 3.0k
Carl A. Busacca United States 28 2.3k 1.2× 840 1.1× 611 1.4× 117 0.5× 195 1.0× 103 2.8k
Simon Woodward United Kingdom 34 3.1k 1.6× 1.5k 1.9× 602 1.3× 392 1.7× 131 0.7× 182 3.8k
Gregory L. Beutner United States 28 3.5k 1.7× 1.0k 1.3× 666 1.5× 119 0.5× 169 0.9× 56 3.9k
Yusuke Kobayashi Japan 28 2.2k 1.1× 438 0.6× 500 1.1× 280 1.2× 88 0.5× 138 2.8k
Olalla Nieto Faza Spain 29 1.8k 0.9× 415 0.5× 220 0.5× 222 0.9× 97 0.5× 94 2.2k
Markus Leutzsch Germany 35 2.7k 1.4× 1.3k 1.6× 382 0.8× 291 1.2× 118 0.6× 131 3.4k

Countries citing papers authored by Jordi Burés

Since Specialization
Citations

This map shows the geographic impact of Jordi Burés's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Jordi Burés with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jordi Burés more than expected).

Fields of papers citing papers by Jordi Burés

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jordi Burés. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Jordi Burés. The network helps show where Jordi Burés may publish in the future.

Co-authorship network of co-authors of Jordi Burés

This figure shows the co-authorship network connecting the top 25 collaborators of Jordi Burés. A scholar is included among the top collaborators of Jordi Burés based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jordi Burés. Jordi Burés is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Procter, Richard J., Dejan-Krešimir Buč̌ar, Henry S. Rzepa, et al.. (2025). Borate-catalysed direct amidation reactions of coordinating substrates. Chemical Science. 16(11). 4718–4724. 2 indexed citations
2.
An, Lan, et al.. (2025). Solvent-free crosslinking of Hydroxypropyl cellulose via esterification: Towards green bioplastics. Carbohydrate Polymers. 371. 124479–124479.
3.
Yang, Xiuxiu, et al.. (2023). Bismuth‐Catalyzed Amide Reduction. Angewandte Chemie International Edition. 62(32). e202306447–e202306447. 10 indexed citations
4.
Burés, Jordi & Igor Larrosa. (2023). Organic reaction mechanism classification using machine learning. Nature. 613(7945). 689–695. 84 indexed citations
5.
Rzepa, Henry S., et al.. (2022). A computational tool to accurately and quickly predict 19 F NMR chemical shifts of molecules with fluorine–carbon and fluorine–boron bonds. Physical Chemistry Chemical Physics. 24(34). 20409–20425. 8 indexed citations
6.
Burés, Jordi, et al.. (2022). Organocatalytic Enantioselective α-Bromination of Aldehydes with N-Bromosuccinimide. The Journal of Organic Chemistry. 87(12). 7968–7974. 4 indexed citations
7.
Burés, Jordi, et al.. (2022). Mechanistic interpretation of orders in catalyst greater than one. Nature Reviews Chemistry. 7(1). 26–34. 22 indexed citations
8.
Burés, Jordi, et al.. (2021). Mechanistically Guided Design of an Efficient and Enantioselective Aminocatalytic α-Chlorination of Aldehydes. Journal of the American Chemical Society. 143(18). 6805–6809. 26 indexed citations
9.
Nielsen, Christian D.‐T., et al.. (2021). Understanding the Diastereopreference of Intermediates in Aminocatalysis: Application to the Chiral Resolution of Lactols. The Journal of Organic Chemistry. 86(5). 4326–4335. 1 indexed citations
10.
Muuronen, Mikko, et al.. (2020). Dual H-bond activation of NHC–Au(i)–Cl complexes with amide functionalized side-arms assisted by H-bond donor substrates or acid additives. Chemical Communications. 56(93). 14697–14700. 26 indexed citations
11.
Clayton, Adam D., Richard A. Bourne, Anna Codina, et al.. (2019). Kinetic Treatments for Catalyst Activation and Deactivation Processes based on Variable Time Normalization Analysis. Angewandte Chemie. 131(30). 10295–10299. 13 indexed citations
12.
Nielsen, Christian D.‐T., Andrew J. P. White, David Sale, Jordi Burés, & Alan C. Spivey. (2019). Hydroarylation of Alkenes by Protonation/Friedel–Crafts Trapping: HFIP-Mediated Access to Per-aryl Quaternary Stereocenters. The Journal of Organic Chemistry. 84(22). 14965–14973. 26 indexed citations
13.
Clayton, Adam D., Richard A. Bourne, Anna Codina, et al.. (2019). Kinetic Treatments for Catalyst Activation and Deactivation Processes based on Variable Time Normalization Analysis. Angewandte Chemie International Edition. 58(30). 10189–10193. 56 indexed citations
14.
15.
Somerville, Rosie J., Lillian V. A. Hale, Enrique Gómez‐Bengoa, Jordi Burés, & Rubén Martı́n. (2018). Intermediacy of Ni–Ni Species in sp2 C–O Bond Cleavage of Aryl Esters: Relevance in Catalytic C–Si Bond Formation. Journal of the American Chemical Society. 140(28). 8771–8780. 86 indexed citations
16.
Muuronen, Mikko, et al.. (2017). Gold(I)-Catalyzed 1,3-O-Transposition of Ynones: Mechanism and Catalytic Acceleration with Electron-Rich Aldehydes. ACS Catalysis. 8(2). 960–967. 11 indexed citations
17.
Burés, Jordi. (2017). What is the Order of a Reaction?. Topics in Catalysis. 60(8). 631–633. 34 indexed citations
18.
Burés, Jordi, Paul Dingwall, Alan Armstrong, & Donna G. Blackmond. (2014). Rationalization of an Unusual Solvent‐Induced Inversion of Enantiomeric Excess in Organocatalytic Selenylation of Aldehydes. Angewandte Chemie International Edition. 53(33). 8700–8704. 30 indexed citations
19.
Bastida, David, et al.. (2011). Gold(III) Complexes Catalyze Deoximations/Transoximations at Neutral pH. Angewandte Chemie International Edition. 50(14). 3275–3279. 22 indexed citations
20.
Burés, Jordi, et al.. (2008). Seebach’s oxazolidinone is a good catalyst for aldol reactions. Tetrahedron Letters. 49(37). 5414–5418. 42 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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